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NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Genetic Test is a sophisticated diagnostic assessment offered by DNA Labs UAE. This test is specifically designed to identify mutations in the NHEJ1 gene, which are known to cause a rare and complex condition characterized by severe combined immunodeficiency (SCID), microcephaly, growth retardation, and increased sensitivity to ionizing radiation. SCID is a critical disorder that severely impairs the body’s immune system, making it highly susceptible to infections. Microcephaly and growth retardation are indicative of developmental issues, while sensitivity to ionizing radiation suggests an increased risk of damage from exposure to certain types of radiation.

Priced at 4400 AED, this genetic test provides invaluable insights for affected individuals and their families, facilitating early intervention and tailored management strategies to mitigate the condition’s impact. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test involves analyzing the patient’s DNA to detect mutations in the NHEJ1 gene, which plays a crucial role in DNA repair and the immune response. Early detection through this genetic test can lead to better outcomes by enabling healthcare providers to devise personalized treatment plans, including gene therapy, immune system management, and protective measures against radiation exposure.

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NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation Genetic Test

Are you concerned about severe combined immunodeficiency (SCID) with microcephaly, growth retardation, and sensitivity to ionizing radiation? DNA Labs UAE offers the NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation Genetic Test to provide you with the answers you need.

Test Details

The NHEJ1 gene is associated with a rare genetic disorder known as severe combined immunodeficiency (SCID) with microcephaly, growth retardation, and sensitivity to ionizing radiation. This disorder is characterized by a weakened immune system, resulting in a high susceptibility to infections. Individuals with this condition also experience abnormal brain development, leading to microcephaly (small head size) and intellectual disability. Additionally, they may exhibit growth retardation and are particularly sensitive to the damaging effects of ionizing radiation.

NGS genetic testing refers to next-generation sequencing, a high-throughput DNA sequencing method that allows for the analysis of multiple genes simultaneously. This type of testing can help identify specific genetic variations or mutations in the NHEJ1 gene that may be responsible for the observed symptoms in individuals suspected to have this disorder. By detecting these genetic abnormalities, NGS genetic testing can aid in confirming a diagnosis, providing information for genetic counseling, and potentially guiding treatment options.

Test Components and Price

The NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation Genetic Test is priced at 4400.0 AED. The test components include:

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Osteology Dermatology Immunology Disorders

Doctor and Test Department

This test is conducted by a dermatologist and falls under the Genetics department at DNA Labs UAE.

Pre Test Information

Prior to undergoing the NHEJ1 Gene Severe Combined Immunodeficiency with Microcephaly Growth Retardation and Sensitivity to Ionizing Radiation Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with this disorder. This information can help in the accurate interpretation of the test results.

Test Name NHEJ1 Gene Severe combined immunodeficiency with microcephaly growth retardation and sensitivity to ionizing radiation Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for NHEJ1 Gene Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NHEJ1 Gene Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation NGS Genetic DNA Test gene NHEJ1
Test Details

The NHEJ1 gene is associated with a rare genetic disorder known as severe combined immunodeficiency (SCID) with microcephaly, growth retardation, and sensitivity to ionizing radiation. This disorder is characterized by a weakened immune system, resulting in a high susceptibility to infections. Individuals with this condition also experience abnormal brain development, leading to microcephaly (small head size) and intellectual disability. Additionally, they may exhibit growth retardation and are particularly sensitive to the damaging effects of ionizing radiation.

NGS genetic testing refers to next-generation sequencing, a high-throughput DNA sequencing method that allows for the analysis of multiple genes simultaneously. This type of testing can help identify specific genetic variations or mutations in the NHEJ1 gene that may be responsible for the observed symptoms in individuals suspected to have this disorder. By detecting these genetic abnormalities, NGS genetic testing can aid in confirming a diagnosis, providing information for genetic counseling, and potentially guiding treatment options.

SKU: TEST-3250 Category:

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